ClinVar Miner

Submissions for variant NM_004595.5(SMS):c.261C>G (p.Asp87Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Revvity Omics, Revvity RCV003138550 SCV003822028 uncertain significance Syndromic X-linked intellectual disability Snyder type 2021-05-08 criteria provided, single submitter clinical testing

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